Reaction Time Conditions Research Articles

The effect of internal and external visualization of rotation on postural stability

IntroductionDuring mental rotation tasks, it is assumed that participants visualize a rotation of objects in their minds (internal visualization), but mental rotation has also been linked to the visible rotation of objects on a screen (external visualization). The angular disparity in mental rotation also influences postural sway, the movements of the body center. Postural sway is thus suspected as one type of indirect measurement of the rotation process. We compare the external visualization of rotation with the suspected internal visualization during mental rotation tasks. We suspect both are similar and thus produce a comparable effect on postural sway.MethodsOne hundred and fifty participants completed three rotation tasks with cube figures, two of which were aided by external visualization. Their center of pressure was measured throughout. The effects of external visualization, angular disparity, and their interaction on postural sway were compared using Bayesian statistics and a decision boundary of 3 or 1/3.Results and discussionThe results indicate no differences between conditions for all postural sway parameters. We observe differences between conditions in cognitive load and reaction time. However, as these partially also differ between the two external visualization conditions and do not transfer to differences between the postural sway parameters, the underlying processes in the three conditions are likely similar. Our results support the notion that the visualization of rotation is central to postural sway during mental rotation. This further supports that the rotation process of the external visualization and mental rotation are similar and thus that stimuli are indeed rotated mentally during mental rotation tasks. Our results further support that the common process between mental and manual rotation lies in the visualization instead of mental rotation being an imagined motor action. Because visual control and feedback play an essential role in many motor tasks, the results could also be of further interest for a more general link between motor and cognitive tasks and bidirectional benefits through the construction of visual similarities.

Comparison of the Effects of Stirring and Standing on Chemical Reactions

AbstractFor hundreds of years, it seems that people have needed stirring to conduct chemical experiments. This operation can be seen everywhere in chemical, pharmaceutical, and materials laboratories and factories. People generally believe that stirring helps with processes such as material dispersion, dissolution, and collision, thereby enabling more-efficient reactions. However, why do chemical reactions that occur in Nature not require stirring? What are the facts? For this purpose, we investigated a total of 329 organic chemical reactions in eight categories and 25 types, including 26 chemical reactions magnified to gram or even kilogram levels. Under the same conditions of temperature, humidity, pressure, and reaction time, we compared the reaction yields under stirring and standing conditions. More than 600 results showed that stirring or not stirring had almost no effect on the efficiency of chemical reactions in solution. If most chemists performing reactions turned off the agitator, it would not be difficult to imagine how much electricity could be saved!

Study on gas–liquid sulfonation reaction under annular flow pattern in micro-reactor: Mechanism, model and process optimization

Micro-sulfonation is a new sulfonation method with great development potential. The gas–liquid micro-sulfonation are safe, efficient and low-cost, however, limited by the research progress and application scope of micro-reactors, the development of gas–liquid micro-sulfonation technique is far from enough. The gas–liquid sulfonation reaction process under annular flow pattern in micro-reactor is experimentally studied in this paper. The maximum MESA (fatty acid methyl ester sulfonic acid) yield under the experimental conditions in this study achieves 89.771 %, which is obviously higher than that (64.1 % for gas–liquid sulfonation and 76.82 % for liquid–liquid sulfonation) in conventional reactors and should be higher if the micro-reactor structure or operating conditions being further optimized. Based on the analyses of experimental results, the effect mechanisms of mass transfer and reaction on the gas–liquid micro-sulfonation efficiency are explored, and the sulfonation efficiency models and pressure drop model of four micro-reactors are established by dimensional analysis method. On account of both the mass transfer characteristics of gas–liquid two-phase flow and the high-viscosity of sulfonation products, enhancing the local disturbance of liquid phase can significantly improve the reaction efficiency. Finally, the operating conditions of two-phase flow rates and reaction time are optimized to ensure the high sulfonation product yield meanwhile reduce the fluid pressure drop or energy consumption of sulfonation process using the improved NSGA-II algorithm.

The synthesis of Fe3O4@SiO2-NNO-CuII nanocatalyst and investigation of its application in the synthesis of imidazo[1,2-a]pyridines

In this study, a tridentate Schiff base ligand obtained from the condensation of salicylaldehyde and 3-amino-1,2,4 triazole was covalently immobilized on the surface of 3-chloro-trimethoxysilane-functionalized magnetic nanoparticles. This nitrogen and oxygen-rich compound provides donor arms for the coordination of copper ions. The prepared nanocatalyst (Fe3O4@SiO2-NNO-CuII) has been characterized by various techniques including FT-IR, EDX, SEM, VSM, XRD and ICP analysis and used as an efficient recyclable catalyst for the synthesis of imidazo[1,2-a]pydidines. Imidazo[1,2-a]pyridine products were obtained through the coupling reaction of substituted benzaldehydes, 2-aminopyridine derivatives and phenylacetylene under solvent-free conditions in high yields and short reaction times.

The Effect of Meal Frequency and Glycemic Index During the Night Shift on Alertness, Hunger, and Gastrointestinal Complaints in Female Health Care Workers—A Two-Armed Randomized Crossover Trial

BackgroundNutrition strategies for night-shift workers could optimize alertness and minimize hunger and reduce gastrointestinal complaints, enhancing safety and well-being. ObjectivesThis study aimed to investigate the effects of 1 or 3 small meals, with either low or high glycemic index (GI), compared with no meal, on alertness, hunger, and gastrointestinal complaints during the night shift. MethodsFifty-one female health care workers, aged 18 to 61 Y, participated in a 2-armed randomized crossover design. In 1 study arm, participants received 1 yogurt meal during the night shift, AND in the other, they received 3. Each study arm involved 3 intervention periods during night shifts, with participants consuming yogurt with low GI (1LGI or 3LGI) OR high GI (1HGI or 3HGI) carbohydrates, or no meal (0NGI). Objective alertness was assessed using a validated brief psychomotor vigilance task (PVT-B), subjective alertness with the Samn–Perelli scale, and hunger and gastrointestinal complaints through questionnaires. ResultsParticipants in the 1LGI (β: −4.6; 95% CI: 0.0, 9.3) and 3LGI (β: −3.4; 95% CI: 0.0, 6.8) conditions had fewer lapses during the PVT-B than those in the 3HGI condition. No differences were found between meal conditions for median and reciprocal reaction time or subjective alertness. All 4 conditions reported less hunger (β: from −0.6 to −1.2) compared with no meal. The 3LGI condition resulted in more rumbling intestines than the 3HGI (β: 1.1; 95% CI: 0.4, 1.7) and 0NGI (β: 0.74; 95% CI: 0.11, 1.37) conditions. ConclusionsOur study suggests that consuming 3 small low GI meals during the night shift helps maintain alertness and reduces lapses compared with 3 high GI meals. It also minimizes hunger but may cause mild gastrointestinal complaints.This trial was registered at International Clinical Trial Registry (https://trialsearch.who.int/Trial2.aspx?TrialID%3dNL-OMON25574).

Optimisation of Catalytic Oxidation Conditions for the 2‐Keto‐L‐Gulonic Acid Production Using Response Surface Methodology

AbstractL‐Ascorbic acid, also known as vitamin C, is a very important antioxidant ingredient situated many usage areas in different industries. 2‐keto‐L‐gulonic acid (2‐KLG) is the main precursor component of L‐ascorbic acid production and it can be produced from L‐sorbose via microbial fermentation or chemical (catalytic) oxidation. While some special strains are used in microbial fermentation, it is benefitted from some catalysts in chemical oxidation. Herein, it was aimed to determine the optimum reaction temperature, pH, and time conditions to produce maximum 2‐KLG compound with the catalytic oxidation of L‐sorbose in the presence of Pt/Al2O3 catalyst with response surface methodology approach. For this aim, the reaction temperature, pH, and time used as variable factors. The limit values of variable factors were applied as 40–60 °C for the temperature, 7.00–9.00 for the pH value, and 3–9 h for the time. The analyses results demonstrated that the increasing temperature and time negatively effected the conversion of L‐sorbose into the 2‐KLG. The optimum conditions of variable factors were determined as 41.30 °C for the temperature, 8.23 for the pH, and 3.25 h for the reaction time by the central composite design. Under these optimum conditions, L‐sorbose was converted into 2‐KLG with an average yield of 43.70 %.

Optimization of Papain Enzyme Activity Using a Response Surface Methodology Approach

Enzyme-based leather dehairing has become widely recognized as a more environmentally friendly alternative to conventional chemical processes. In recent decades, the demand for plant-based enzymes has grown, leading to the need to improve catalytic efficiency and meet industrial requirements through advanced extraction and isolation techniques. Therefore, the objective of this study was to extract plant papain enzyme from <i>Carica papaya</i> and evaluate their potential as a dehairing agent in the leather industry. The experimental study was conducted in a laboratory setting from July to August 2023. <i>Carica papaya</i> samples were collected from various locations in Arba Minch town. Papain enzyme was extracted from <i>Carica papaya</i> by grinding it in a blender with extraction media such as distilled water and 50 mM phosphate buffers. The optimization of proteolytic activity was performed using the response surface method and Box-Behnken Design (BBD), considering parameters like pH, temperature, and reaction time. The optimized conditions for temperature, pH, and reaction time were found to be 55°C, 7.5, and 38.5 minutes, respectively, resulting in an optimum protease activity of 32 U/ml. The crude protease enzyme derived from papaya was successfully used to dehair goat hides at 25°C for 16 hours without the addition of Na<sup>2</sup>S. Microscopic analysis revealed hides that were free of epidermis and hair, with clean pores and no significant damage to the grain surface. In conclusion, the papain enzyme derived from <i>Carica papaya</i> can be a valuable tool for implementing cleaner technologies in tanneries, particularly for lime and sulphide-free dehairing processes.

Enhanced diclofenac adsorption and degradation using iron‐loaded modified spent bleaching earth carbon in the presence of clofibric acid: mechanistic insights and toxicity assessment

AbstractBACKGROUNDThe presence of pharmaceutical active substances such as diclofenac (DCF) and clofibric acid (CA) in aquatic environments poses significant ecological threats. Existing treatments have not fully explored the impact of CA on DCF removal efficiency. This research introduces nZVI/CTAB‐SBE@C, a novel adsorbent developed from industrial spent bleaching earth (SBE), modified with cetyltrimethylammonium bromide (CTAB) and nano zero‐valent iron (nZVI), enhancing both adsorption and degradation of DCF and CA.RESULTSThis study investigated the impact of CA on the removal capabilities of nZVI/CTAB‐SBE@C for DCF in a coexisting system. Systematic examinations were conducted on the effects of various parameters, including reaction time, dosage, temperature, actual wastewater, humic acid content and coexisting ions. Results indicated that the presence of CA significantly enhanced the DCF removal efficiency, achieving an optimal rate of 87.3% under conditions of reaction time 2 h, adsorbent dosage 5 g L−1 and temperature 25 °C. Moreover, interactions between Al3+ ions and the adsorbent matrix notably improved removal efficiencies for both DCF and CA. Analysis revealed that CA facilitated new degradation pathways for DCF, including hydroxylation and decarboxylation reactions. Additionally, the presence of CA reduced the toxicity of degradation intermediates, enhancing environmental safety compared to systems containing only DCF.CONCLUSIONThis study effectively transforms industrial waste into the efficient nZVI/CTAB‐SBE@C adsorbent. The presence of CA not only boosts DCF removal efficiency but also promotes its safer degradation, thereby reducing the ecological impact of contaminants. © 2024 Society of Chemical Industry (SCI).

Preparation and characterization of ion-exchanged Ni-Na-β”-Al2O3 and Fe-Na-β”-Al2O3 solid electrolytes for applications in liquid metals

Accurate determinations of the thermochemical properties for the steel alloying elements (Fe, Cr, Ni, Co and Mn) dissolved as corrosion product impurities in Pb and Pb–Bi alloy (LBE) are relevant for the development of Lead-Cooled Fast Nuclear Reactors (LFRs). Ion-selective solid electrolytes are suitable for an electrochemical characterization of the dissolved impurities. Among these, ion-exchanged Ni-β”-Al2O3 and Fe-β”-Al2O3 are promising solid electrolytes for the selective detection of Ni and Fe dissolved in HLMs. In the present works we proposed a preliminary test of liquid and vapor ion-exchanges on commercial polycrystalline Na-β”-Al2O3 tubes at different conditions of temperature and reaction time with NiCl2 and FeCl2 salts, characterizing the effects on the material microstructure. The resulting Ni-Na-β”-Al2O3 and Fe-Na-β”-Al2O3 samples were only partially replaced by nickel or iron, extremely porous, damaged by molten salt corrosion, and contaminated by residual chlorides. When tested as selective sensors in molten LBE, they failed in detecting dissolved nickel or iron. Thus, ion-exchange procedure on polycrystalline Na-β”-Al2O3 substrates still needs to be improved by properly combining the liquid and vapor ion-exchange with optimized reaction conditions in order to increase the sodium replacement yield. Alternatively, efforts may be focused on the preparation and application of other different nickel and iron solid electrolytes.

Electrochemically assisted preparation of graphitic carbon nitride nanosheet membranes for efficient water purification

The development of a highly effective nanofiltration membrane for water purification is crucial for wastewater recovery. The graphitic carbon nitride (g-C3N4) membrane can be an ideal candidate for advanced water treatment due to its intrinsic porous structure and superior physicochemical stability. However, the developments of the g-C3N4 membranes are limited by their traditional preparation methods involving complicated processes, long reaction time and high-temperature conditions. A simple electrochemical-assisted strategy for the rapid preparation of the g-C3N4 nanosheet membranes at room temperature has been developed in this study. The ultra-thin g-C3N4 membrane with a uniform structure can be synthesized within 40 min, which is at least 7 times quicker compared to the traditional methods. The as-prepared g-C3N4 membrane shows a high water flux rate of ∼ 90 L m−2 h−1 bar−1. Simultaneously, an excellent rejection rate of 99.1% toward Evans blue is achieved based on the synergistic effect of size sieving and electrostatic repulsion. The breakthrough in the preparation method of g-C3N4 nanosheet membranes in this work is of great significance to the development of g-C3N4 membranes in the field of water purification.

Synthesis of spiro-oxindole-based chemosensor for detection of Hg2+ ions using SBA-Pr-N-IS-Bu-SO3H

Spiro-oxindoles were prepared efficiently via multicomponent reactions (MCRs) for finding the new chemosensors. Also, the use of the efficient nanocatalysts based on SBA-15 in these reactions are so important. Therefore, the functionalization of SBA-15 by different organic compounds are common to produce new efficient nanocatalysts. Herein, SBA-Pr-N-Is-Bu-SO3H as an efficient nanoporous catalyst was applied in the synthesis of (5,6,7,8-tetrahydro-chromene)-4,3′-spirocyclic oxindoles through the three-component reaction of isatin derivatives, malononitrile and dimedone under reflux conditions in high yield and short reaction time. Among all spiro-oxindole derivatives, 2-amino-7,7-dimethyl-5′-nitro-2′,5-dioxo-5,6,7,8-tetrahydro-spiro[chromen-4,3′-indoline]-3-carbonitrile was investigated in fluoresence spectroscopy. According to the obtained results it was observed that in the presence of various cations such as, K+, Ca2+, Na+, Cu2+, Zn2+, Cr3+, Fe3+, Fe2+, Mn2+, Co2+, Al3+, Pb2+, Ag+, Cd2+, Ni2+, Hg2+ and Mg2+, it can selectively detect Hg2+ ion and increase the emission intensity. Its calculated detection limit was 4.6 × 10−7 M, which can be considered a good value. Also, in order to determine the stoichiometric ration for ligand and Hg2+ ion, Job's plot test was performed and the ratio was 1:2.

Ultrasound-assisted nano-GO/NiO mediated green synthesis, DFT studies and antiinflammatory activity of spiro indoles

An improved procedure has been developed for synthesizing derivatives of spiroindole in 84–87% yield by using catalytic amount of graphene oxide supported nickel oxide nanocomposite (GO/NiO NC) as a proficient heterogeneous catalyst under ultrasonic-irradiation. GO/NiO NC can be recycled and reused for three successive runs with slight reduction in its catalytic activity. Short reaction time, simple workup, and eco-friendly conditions are key features of the current protocol. Most importantly, the synthesized compounds, 4b, 4c, 5b, 5c, and 5d showed good anti-inflammatory potential by inhibiting protein denaturation at all the given concentrations. HOMO-LUMO studies indicate that the carbonitrile derivatives have the smallest energy gap which implies more chemical reactivity.

A pre-screening of the solvolysis recycling process for CFRPs based on the mechanical properties of the recovered fibers.

Over the past few decades, composite materials, and specifically carbon fiber reinforced plastics (CFRPs), are finding increasing use in the automotive, aerospace, and aeronautics industries. As a result, the production of CFRPs has been significantly increased, thus leading to a corresponding increase in waste production. In the near future, landfill and incineration disposal of waste will likely be prevented due to legislation, thereby bringing forward the need to develop efficient recycling processes for CFRPs. However, recycling of CFRPs is very challenging, mainly due to the difficulty in removing the thermosetting matrix. This paper reports a pre-screening of the solvolysis recycling process for CFRPs on the basis of the mechanical properties of the recovered fibers. To this end, solvolysis tests were conducted on unidirectional CFRP samples under supercritical and subcritical conditions using acetone and water. The solvolysis tests were conducted for various conditions of temperature, pressure, and reaction time. The efficiency of the recycling processes has been evaluated by means of single-fiber tension tests on the recovered fibers, which were conducted according to the ASTM C 1557-14 standard. In most cases, the decomposition efficiency of the epoxy resin in the CFRP, measured in terms of mass, ranged between 90 and 100%. Moreover, the mechanical tests showed that the recovered fibers retained more than 58% of their initial Young’s modulus and tensile strength.

A Preliminary Investigation on a Water- and Acetone-Based Solvolysis Recycling Process for CFRPs.

Composites, and especially carbon-fiber-reinforced plastics (CFRPs), are increasingly used in the automotive, aerospace, and aviation industries, and as a result, CFRP production has increased dramatically, leading to a corresponding increase in waste. Landfills and the incineration of waste are likely to be restricted as a result of legislation, thus highlighting the need for efficient recycling methods for CFRPs. However, the recycling of CFRPs is very challenging, mainly due to the difficulty of removing their thermosetting matrix. This study reports a pre-screening of the solvolysis recycling process for CFRPs based on the mechanical properties of the recovered fibers. To this end, solvolysis tests were conducted on unidirectional CFRP samples under supercritical and subcritical conditions using acetone and water. The solvolysis tests were conducted for various conditions of temperature, pressure, and reaction time, without the use of any catalyst. Also, the loading rate (volume of solvent/volume of reactor) was constant. The efficiency of the recycling processes has been evaluated through a morphological and a mechanical characterization of the recovered fibers. In most cases, the decomposition efficiency of the epoxy resin, measured in terms of mass, ranged between 90 and 100%. Moreover, the scanning electron microscopy images of the recovered fibers showed negligible traces of resin residues and no detectable signs of physical damage or any changes in morphology with regard to diameter. Finally, the single-fiber tension tests revealed that that the recovered fibers retained more than 61% of their initial Young's modulus and 70% of their tensile strength.

An efficient four-component protocol for synthesis of poly-substituted pyridines with SiO2 as a robust recyclable catalyst

A four-component protocol for the development of poly-substituted pyridines derivatives by using SiO2 as a recycle catalyst. The protocol offers good to excellent yields (85%-95%) under milder conditions in a short reaction time of 2-3 hours. The use of a less expensive catalyst makes this protocol more convenient. SiO2 has been identified as a convenient catalyst for the synthesis and can be reused for up to three cycles.

Novel green protocols for the synthesis of tetrahydropyrazolopyrazolones

1,3 – Dipolar cycloadditions represent an important method for obtaining novel bicyclic heterocycles which is of great importance due to their medicinal application and diverse bioactivity such as antitumor, antibacterial and etc. The most suitable way for the synthesis of bicyclic heterocycles such as pyrazolopyrazolones is based on dipolar cycloaddition of azomethine imines and enones. This reaction was explored to develop more sustainable protocols by using less toxic chemicals and different sources of energy. Herein novel green protocols for the synthesis of tetrahydropyrazolopyrazolones are presented. These green protocols avoid hazardous AlCl3 and CH2Cl2 which were used until now, and implement green sources of irradiation. In this research, acetic acid has proved itself as a great catalyst for this type of reaction. Different azomethine imines and enones were submitted to the reaction in the presence of acetic acid for 12 h. A series of ten tetrahydropyrazolopyrazolones is successfully synthesized. The impact of ultrasound and microwave irradiation was also investigated. Three novel protocols for the synthesis of tetrahydropyrazolopyrazolones were established. The best results with significant improvement in yield, reaction time, and cleaner reaction conditions were observed when acetic acid and microwave irradiation were used. These novel protocols for the synthesis of pyrazolopyrazolones based on the usage of acetic acid as a catalyst and ultrasound and microwave irradiation represent a noteworthy advancement in research of sustainable methods for obtaining heterocycles.

Facile synthesis of spiro-pyrazolone-tetrahydrofurans/pyrans: ipso-cyclization of arylidene pyrazolones with haloalcohols

Facile synthesis of spiro-pyrazolone-tetrahydrofurans & pyrans by base-mediated cascade ipso-cyclization of haloalcohols & arylidine pyrazolones is realised. Features include brief reaction time, practicality, good yields and mild reaction conditions.

Structures, dielectric properties and AC impedance characteristics of BiFeO3–BaTiO3 high-temperature lead-free piezoceramics synthesized by the hydrothermal method

Among the lead-free piezoceramics, ([Formula: see text])BiFeO[Formula: see text]BaTiO3 (BF-BT) is considered a promising candidate for high-temperature piezoelectric materials owing to its high Curie temperature ([Formula: see text]C) and good electromechanical properties. In this work, the hydrothermal synthesis method was used to prepare the precursor powders of BiFeO3 and BaTiO3, and then the mixed powder compacts with the chemical composition of 0.7BF–0.3BT were sintered under pressureless conditions. The influence of the hydrothermal reaction times (12–24[Formula: see text]h) of BiFeO3 on the structures and electric properties of the sintered ceramics was instigated. First, all the samples synthesized with the tetragonal BaTiO3 and BiFeO3 powders were identified with relatively stable dielectric properties. As the hydrothermal reaction time to synthesize BiFeO3 increased, the dielectric properties as well as the temperature stability of the 0.7BiFeO3–0.3BaTiO3 ceramics also improved. At the condition of a hydrothermal reaction time of 24[Formula: see text]h, the sample obtained possesses both the lowest temperature coefficient of dielectric constant ([Formula: see text]C between RT and [Formula: see text]C) and the highest Curie temperature ([Formula: see text]C at 100[Formula: see text]kHz). Moreover, at high temperatures, it exhibits a higher AC impedance than others. The calculating result based on the resistive constant-phase-element model (R-CPE) circuit model showed that the grain boundary of the 0.7BF–0.3BT ceramics contributes more resistance to the conductivity at high temperatures. In summary, the hydrothermal reaction proved to be a useful way that achieves the preparation of single-phase 0.7BF–0.3BT ceramics with improved electrical properties.

MgAl2O4 nanospinel: Green synthesis, characterization and effective heterogeneous catalyst for the photocatalytic degradation of carbol fuchsin dye and synthesis of 2-aryl substituted benzoxazole derivatives

In this study we report, plant extract mediated green, expedient, cost effective and environment friendly synthesis of MgAl2O4 nanospinel and their potential application in the field of photocatalytic degradation of organic contaminant and biologically active benzoxazole synthesis. The synthesized spinel material was characterized by XRD, TGA, FT-IR, FE-SEM, EDAX, TEM, UV–Visible spectra, XPS and BET for obtaining the structural, morphological, optical, and textural properties. Sunlight driven photocatalytic degradation efficiency of this catalyst was performed on a widely used industrial dye carbol fuchsin (CF) which is a major contaminant that is being mixed in water resources. The contamination could be degraded upto 96.84 % when its concentration is 30 ppm at pH 9, by the nanospinel of 0.6 g/L. Kinetic model of degradation follows pseudo- first order kinetic with rate constant of 0.043 min−1. Also the nanospinel has the key benefits in the synthesis of some benzoxazole derivatives as a catalyst, that its shorter reaction time, excellent yield, safety and moderate reaction conditions, non-toxicity and simple work up procedures.

Synthesis of a Grease Thickener from Cashew Nut Shell Liquor.

Thickener, also known as a gelling agent, is a critical component of lubricating greases. The most critical property of thickener, temperature resistance, is determined by the molecular structure of the compounds. Currently, all high-temperature-resistant thickeners are based on 12-hydroxystearic acid, which is exclusively produced from castor oil. Since castor oil is also an important reagent for other processes, finding a sustainable alternative to 12-hydroxystearic acid has significant economic implications. This study synthesises an alternative thickener from abundant agricultural waste, cashew nut shell liquor (CNSL). The synthesis and separation procedure contains three steps: (i) forming and separating calcium anacardate by precipitation, (ii) forming and separating anacardic acid (iii) forming lithium anacardate. The obtained lithium anacardate can be used as a thickener for lubricating grease. It was found that the recovery of anacardic acid was around 80%. The optimal reaction temperature and time conditions for lithium anacardate were 100 °C and 1 h, respectively. The method provides an economical alternative to castor and other vegetable oils. The procedure presents a simple pathway to produce the precursor for the lubricating grease from agricultural waste. The first reaction step can be combined with the existing distillation of cashew nut shell processing. An effective application can promote CNSL to a sustainable feedstock for green chemistry. The process can also be combined with recycled lithium from the spent batteries to improve the sustainability of the battery industry.